Schlensog V, Böck A
Lehrstuhl für Mikrobiologie der Universität, München, FRG.
Mol Microbiol. 1990 Aug;4(8):1319-27. doi: 10.1111/j.1365-2958.1990.tb00711.x.
Through complementation of a trans-acting regulatory mutation a gene has been cloned whose product is required for the formate induction of the anaerobic expression of the formate hydrogenlyase structural genes. By restriction analysis, and from the size of the encoded protein, the gene could be identified as being equivalent to fhlA described by Sankar et al. (1988). The nucleotide sequence of the fhlA gene was determined and it was shown to code for a protein with a calculated Mr of 78,467. Analysis of the derived amino acid sequence showed that the carboxy-terminal domain of FHLA shares considerable sequence similarity with NIFA and NTRC, which are the 'regulators' of two-component regulatory systems. Carboxy-terminal truncation of, and introduction of amino-terminal deletions in, the fhlA gene delivered inactive gene products. When overexpressed, FHLA mediates activation of expression of the formate dehydrogenase and hydrogenase structural genes in the presence of formate also under aerobic growth conditions. FHLA appears to bind to the upstream regulatory sequence (URS) in the 5' flanking region of the fdhF gene since activation of fdhF expression was dependent on the presence of the URS.
通过对一个反式作用调节突变进行互补,克隆了一个基因,其产物是甲酸氢化酶结构基因厌氧表达的甲酸诱导所必需的。通过限制性分析以及根据编码蛋白的大小,该基因可被鉴定为与桑卡尔等人(1988年)描述的fhlA等同。测定了fhlA基因的核苷酸序列,结果表明它编码一种计算分子量为78467的蛋白质。对推导的氨基酸序列的分析表明,FHLA的羧基末端结构域与NIFA和NTRC有相当大的序列相似性,NIFA和NTRC是双组分调节系统的“调节因子”。fhlA基因的羧基末端截短以及氨基末端缺失的引入产生了无活性的基因产物。当过量表达时,FHLA在有氧生长条件下也能在甲酸存在的情况下介导甲酸脱氢酶和氢化酶结构基因表达的激活。FHLA似乎与fdhF基因5'侧翼区域的上游调节序列(URS)结合,因为fdhF表达的激活依赖于URS的存在。